Description

1H-Pyrrole,2,5-Dihydro-1,2-Dimethyl-3-(2-Naphthalenyl)-,(2S)-(9Ci) is a chiral, substituted pyrrolidine derivative of significant interest in advanced organic synthesis. This compound matters as a sophisticated building block for the development of novel active pharmaceutical ingredients (APIs) and functional materials. It is primarily needed by research and development teams in the pharmaceutical and agrochemical industries, where its unique stereochemistry and fused ring system enable the creation of complex molecular architectures.

Application

• Pharmaceutical Intermediate: Serves as a key chiral precursor in the synthesis of potential drug candidates, particularly for central nervous system (CNS) targets.
• Agrochemical Research: Used in developing novel pesticides and herbicides, leveraging its naphthalene moiety for bioactivity.
• Ligand Synthesis: Acts as a starting material for creating specialized ligands used in asymmetric catalysis and metal-organic frameworks (MOFs).
• Material Science: Investigated as a monomer or dopant for creating conductive polymers or organic semiconductors.
• Academic & Contract Research: Employed in university and CRO laboratories for methodological studies in heterocyclic and stereoselective chemistry.
• Fine Chemical Production: Utilized in the multi-step synthesis of high-value, complex organic molecules for various industrial applications.

Basic Information

Product Name	1H-Pyrrole,2,5-Dihydro-1,2-Dimethyl-3-(2-Naphthalenyl)-,(2S)-(9Ci)
CAS No.	823178-95-6
Molecular Formula	C₁₇H₁₉N
Molecular Weight	237.34 g/mol
Synonyms	(2S)-1,2-Dimethyl-3-(naphthalen-2-yl)-2,5-dihydro-1H-pyrrole; (S)-1,2-Dimethyl-3-(2-naphthyl)-2,5-dihydro-1H-pyrrole; 2-Naphthalene, 1,2-dihydro-1,2-dimethyl-3-(2-naphthalenyl)-, (2S)-; 823178-95-6; (S)-1,2-Dimethyl-3-(naphthalen-2-yl)-2,5-dihydro-1H-pyrrole; 1H-Pyrrole, 2,5-dihydro-1,2-dimethyl-3-(2-naphthalenyl)-, (2S)-
EINECS	Contact for details

Quality Control

Our products undergo rigorous quality testing to ensure compliance with industry standards. Every batch is characterized using advanced analytical techniques including HPLC, GC, NMR, and chiral analysis to confirm identity, purity, and enantiomeric excess. Certificates of Analysis (COA) detailing all relevant specifications are available upon request. We adhere to a cGMP-compliant quality management system for production and control, ensuring reliability for research and scale-up activities.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at a controlled room temperature (15-25°C) in a cool, dry, and well-ventilated area. This compound is easily oxidized and light-sensitive; prolonged exposure to air or light should be avoided to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Enantiomeric Excess (Chiral HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.